A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699156



Internal ID15089122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75194071..75308948hg38UCSC Ensembl
Innerchr16:75227969..75342846hg19UCSC Ensembl
Innerchr16:73785470..73900347hg18UCSC Ensembl
Innerchr16:73785470..73900347hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38114878
hg19114878
hg18114878
hg17114878
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523405
Supporting Variants
Samples
Known GenesBCAR1, CFDP1, CTRB1, CTRB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699156
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer